Visual function and cortical organization in carriers of blue cone monochromacy.

Carriers of blue cone monochromacy have fewer cone photoreceptors than normal. Here we examine how this disruption at the level of the retina affects visual function and cortical organization in these individuals. Visual resolution and contrast sensitivity was measured at the preferred retinal locus...

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Main Authors: Ethan A Rossi, Rebecca L Achtman, Arnaud Guidon, David R Williams, Austin Roorda, Daphne Bavelier, Joseph Carroll
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3585243?pdf=render
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spelling doaj-5d50671c65374ea3be2fa16dbf8c9d272020-11-25T02:51:32ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0182e5795610.1371/journal.pone.0057956Visual function and cortical organization in carriers of blue cone monochromacy.Ethan A RossiRebecca L AchtmanArnaud GuidonDavid R WilliamsAustin RoordaDaphne BavelierJoseph CarrollCarriers of blue cone monochromacy have fewer cone photoreceptors than normal. Here we examine how this disruption at the level of the retina affects visual function and cortical organization in these individuals. Visual resolution and contrast sensitivity was measured at the preferred retinal locus of fixation and visual resolution was tested at two eccentric locations (2.5° and 8°) with spectacle correction only. Adaptive optics corrected resolution acuity and cone spacing were simultaneously measured at several locations within the central fovea with adaptive optics scanning laser ophthalmoscopy (AOSLO). Fixation stability was assessed by extracting eye motion data from AOSLO videos. Retinotopic mapping using fMRI was carried out to estimate the area of early cortical regions, including that of the foveal confluence. Without adaptive optics correction, BCM carriers appeared to have normal visual function, with normal contrast sensitivity and visual resolution, but with AO-correction, visual resolution was significantly worse than normal. This resolution deficit is not explained by cone loss alone and is suggestive of an associated loss of retinal ganglion cells. However, despite evidence suggesting a reduction in the number of retinal ganglion cells, retinotopic mapping showed no reduction in the cortical area of the foveal confluence. These results suggest that ganglion cell density may not govern the foveal overrepresentation in the cortex. We propose that it is not the number of afferents, but rather the content of the information relayed to the cortex from the retina across the visual field that governs cortical magnification, as under normal viewing conditions this information is similar in both BCM carriers and normal controls.http://europepmc.org/articles/PMC3585243?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Ethan A Rossi
Rebecca L Achtman
Arnaud Guidon
David R Williams
Austin Roorda
Daphne Bavelier
Joseph Carroll
spellingShingle Ethan A Rossi
Rebecca L Achtman
Arnaud Guidon
David R Williams
Austin Roorda
Daphne Bavelier
Joseph Carroll
Visual function and cortical organization in carriers of blue cone monochromacy.
PLoS ONE
author_facet Ethan A Rossi
Rebecca L Achtman
Arnaud Guidon
David R Williams
Austin Roorda
Daphne Bavelier
Joseph Carroll
author_sort Ethan A Rossi
title Visual function and cortical organization in carriers of blue cone monochromacy.
title_short Visual function and cortical organization in carriers of blue cone monochromacy.
title_full Visual function and cortical organization in carriers of blue cone monochromacy.
title_fullStr Visual function and cortical organization in carriers of blue cone monochromacy.
title_full_unstemmed Visual function and cortical organization in carriers of blue cone monochromacy.
title_sort visual function and cortical organization in carriers of blue cone monochromacy.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Carriers of blue cone monochromacy have fewer cone photoreceptors than normal. Here we examine how this disruption at the level of the retina affects visual function and cortical organization in these individuals. Visual resolution and contrast sensitivity was measured at the preferred retinal locus of fixation and visual resolution was tested at two eccentric locations (2.5° and 8°) with spectacle correction only. Adaptive optics corrected resolution acuity and cone spacing were simultaneously measured at several locations within the central fovea with adaptive optics scanning laser ophthalmoscopy (AOSLO). Fixation stability was assessed by extracting eye motion data from AOSLO videos. Retinotopic mapping using fMRI was carried out to estimate the area of early cortical regions, including that of the foveal confluence. Without adaptive optics correction, BCM carriers appeared to have normal visual function, with normal contrast sensitivity and visual resolution, but with AO-correction, visual resolution was significantly worse than normal. This resolution deficit is not explained by cone loss alone and is suggestive of an associated loss of retinal ganglion cells. However, despite evidence suggesting a reduction in the number of retinal ganglion cells, retinotopic mapping showed no reduction in the cortical area of the foveal confluence. These results suggest that ganglion cell density may not govern the foveal overrepresentation in the cortex. We propose that it is not the number of afferents, but rather the content of the information relayed to the cortex from the retina across the visual field that governs cortical magnification, as under normal viewing conditions this information is similar in both BCM carriers and normal controls.
url http://europepmc.org/articles/PMC3585243?pdf=render
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